Rituxan Now Shipping In The USA

18 December 1997

IDEC and Genentech have started shipping Rituxan (rituximab), ananti-CD20 monoclonal antibody for the treatment of relapsed or refractory low-grade or follicular B-cell non-Hodgkin's lymphoma, to oncologists in the USA. The product was approved there earlier this month (Marketletter December 8).

This is the second launch for the product. It was first introduced by Roche in Switzerland a few weeks ago, under the trade name MabThera. The development of rituximab was also undertaken by Zenyaku Kogyo of Japan. In the USA, IDEC and Genentech will copromote the product and share responsibility for its manufacture.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK



Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight